Canonical Allele Identifier: CA1304728016
Gene: GALNT3 HGNC NCBI

Linked Data

dbSNP Id: rs1688286161

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165747811G>C , CM000664.2:g.165747811G>C GRCh38
NC_000002.11:g.166604321G>C , CM000664.1:g.166604321G>C GRCh37
NC_000002.10:g.166312567G>C NCBI36
NG_012069.1:g.51483C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392701.8:c.*970C>G MANE Select ENSP00000376465.3:n.*970C>G
ENST00000392701.7:c.*970C>G ENSP00000376465.3:n.*970C>G
ENST00000409882.5:c.*970C>G ENSP00000386955.1:n.*970C>G
NM_004482.3:c.*970C>G NP_004473.2:n.*970C>G
XM_005246449.1:c.*970C>G XP_005246506.1:n.*970C>G
XM_011510929.1:c.*970C>G XP_011509231.1:n.*970C>G
XM_017003770.1:c.*970C>G XP_016859259.1:n.*970C>G
NM_004482.4:c.*970C>G MANE Select NP_004473.2:n.*970C>G